PubMed

Replication of calpain-10 genetic association with carotid intima-media thickness.

Goodarzi MO, Taylor KD, Jones MR, Fang B, Guo X, Xiang AH, Buchanan TA, Hodis HN, Raffel LJ, Rotter JI.

Atherosclerosis. 2009 Aug;205(2):503-5. Epub 2009 Jan 9.PMID: 19193380 [PubMed - in process]Related articles

Association of insulin sensitivity and glucose tolerance with the c.825C>T variant of the G protein beta-3 subunit gene.

Kopf D, Cheng LS, Blandau P, Hsueh W, Raffel LJ, Buchanan TA, Xiang AH, Davis RC, Rotter JI, Lehnert H.

J Diabetes Complications. 2008 May-Jun;22(3):205-9. Epub 2008 Apr 16.PMID: 18413224 [PubMed - indexed for MEDLINE]Related articlesFree article

HLA on chromosome 6: the story gets longer and longer.

Raffel LJ, Noble JA, Rotter JI.

Diabetes. 2008 Mar;57(3):527-8. No abstract available. PMID: 18305146 [PubMed - indexed for MEDLINE]Related articlesFree article

Carotid intima-media thickness (cIMT) cosegregates with blood pressure and renal function in hypertensive Hispanic families.

Chen YC, Guo X, Raffel LJ, Xiang AH, Fang B, Hsueh WA, Taylor KD, Buchanan TA, Hodis HN, Rotter JI.

Atherosclerosis. 2008 May;198(1):160-5. Epub 2007 Oct 29.PMID: 18028933 [PubMed - indexed for MEDLINE]Related articles

Aryl hydrocarbon receptor interacting protein variants in sporadic pituitary adenomas.

Yu R, Bonert V, Saporta I, Raffel LJ, Melmed S.

J Clin Endocrinol Metab. 2006 Dec;91(12):5126-9. Epub 2006 Oct 3.PMID: 17018653 [PubMed - indexed for MEDLINE]Related articlesFree article

DPB1 alleles are associated with type 1 diabetes susceptibility in multiple ethnic groups.

Cruz TD, Valdes AM, Santiago A, Frazer de Llado T, Raffel LJ, Zeidler A, Rotter JI, Erlich HA, Rewers M, Bugawan T, Noble JA.

Diabetes. 2004 Aug;53(8):2158-63.PMID: 15277401 [PubMed - indexed for MEDLINE]Related articlesFree article

A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes.

Guo D, Li M, Zhang Y, Yang P, Eckenrode S, Hopkins D, Zheng W, Purohit S, Podolsky RH, Muir A, Wang J, Dong Z, Brusko T, Atkinson M, Pozzilli P, Zeidler A, Raffel LJ, Jacob CO, Park Y, Serrano-Rios M, Larrad MT, Zhang Z, Garchon HJ, Bach JF, Rotter JI, She JX, Wang CY.

Nat Genet. 2004 Aug;36(8):837-41. Epub 2004 Jul 11. Erratum in: Nat Genet. 2004 Sep;36(9):1024. PMID: 15247916 [PubMed - indexed for MEDLINE]Related articles

Genetic testing and human subjects in research.

Laidlaw SA, Raffel LJ, Daar JF.

Whittier Law Rev. 2002 Winter;24(2):429-72. No abstract available. PMID: 15085855 [PubMed - indexed for MEDLINE]Related articles

Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element.

Hoogendijk CF, Scholtz CL, Pimstone SM, Ehrenborg E, Kastelein JJ, Defesche JC, Thiart R, du Plessis L, de Villiers JN, Zaahl MG, Delport R, Rubinsztein DC, Raffel LJ, Grim CE, Mediene-Benchekor S, Amouyel P, Brousseau T, Steyn K, Lombard CJ, Hayden MR, Kotze MJ.

Mol Cell Probes. 2003 Aug;17(4):175-81.PMID: 12944120 [PubMed - indexed for MEDLINE]Related articles

Heritability of subclinical atherosclerosis in Latino families ascertained through a hypertensive parent.

Xiang AH, Azen SP, Buchanan TA, Raffel LJ, Tan S, Cheng LS, Diaz J, Toscano E, Quinonnes M, Liu CR, Liu CH, Castellani LW, Hsueh WA, Rotter JI, Hodis HN.

Arterioscler Thromb Vasc Biol. 2002 May 1;22(5):843-8.PMID: 12006400 [PubMed - indexed for MEDLINE]Related articlesFree article

Autoantibodies and human leucocyte antigen class II in first-degree family members of Mexican-American type 1 diabetic patients.

Zeidler A, Raffel LJ, Costin G, Shaw SJ, Buchanan TA, Noble J, Rotter JI, Palmer J, Krischer JP, Wait C, Maclaren NK.

J Clin Endocrinol Metab. 2001 Oct;86(10):4957-62.PMID: 11600569 [PubMed - indexed for MEDLINE]Related articlesFree article

Coincident linkage of fasting plasma insulin and blood pressure to chromosome 7q in hypertensive hispanic families.

Cheng LS, Davis RC, Raffel LJ, Xiang AH, Wang N, Quiñones M, Wen PZ, Toscano E, Diaz J, Pressman S, Henderson PC, Azen SP, Hsueh WA, Buchanan TA, Rotter JI.

Circulation. 2001 Sep 11;104(11):1255-60.PMID: 11551876 [PubMed - indexed for MEDLINE]Related articlesFree article

Evidence for joint genetic control of insulin sensitivity and systolic blood pressure in hispanic families with a hypertensive proband.

Xiang AH, Azen SP, Raffel LJ, Tan S, Cheng LS, Diaz J, Toscano E, Henderson PC, Hodis HN, Hsueh WA, Rotter JI, Buchanan TA.

Circulation. 2001 Jan 2;103(1):78-83.PMID: 11136689 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic and physical mapping of a type 1 diabetes susceptibility gene (IDDM12) to a 100-kb phagemid artificial chromosome clone containing D2S72-CTLA4-D2S105 on chromosome 2q33.

Marron MP, Zeidler A, Raffel LJ, Eckenrode SE, Yang JJ, Hopkins DI, Garchon HJ, Jacob CO, Serrano-Rios M, Martinez Larrad MT, Park Y, Bach JF, Rotter JI, Yang MC, She JX.

Diabetes. 2000 Mar;49(3):492-9.PMID: 10868973 [PubMed - indexed for MEDLINE]Related articlesFree article

Peritoneal serous papillary carcinoma, a phenotypic variant of familial ovarian cancer: implications for ovarian cancer screening.

Karlan BY, Baldwin RL, Lopez-Luevanos E, Raffel LJ, Barbuto D, Narod S, Platt LD.

Am J Obstet Gynecol. 1999 Apr;180(4):917-28.PMID: 10203660 [PubMed - indexed for MEDLINE]Related articles

Early presentation of type 2 diabetes in Mexican-American youth.

Neufeld ND, Raffel LJ, Landon C, Chen YD, Vadheim CM.

Diabetes Care. 1998 Jan;21(1):80-6.PMID: 9538974 [PubMed - indexed for MEDLINE]Related articlesFree article

The epidemiology and genetic basis of common diseases.

Raffel LJ.

Pediatr Ann. 1997 Sep;26(9):525-34. No abstract available. PMID: 9302714 [PubMed - indexed for MEDLINE]Related articles

Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood.

Scheuner MT, Wang SJ, Raffel LJ, Larabell SK, Rotter JI.

Am J Med Genet. 1997 Aug 22;71(3):315-24.PMID: 9268102 [PubMed - indexed for MEDLINE]Related articles

Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups.

Marron MP, Raffel LJ, Garchon HJ, Jacob CO, Serrano-Rios M, Martinez Larrad MT, Teng WP, Park Y, Zhang ZX, Goldstein DR, Tao YW, Beaurain G, Bach JF, Huang HS, Luo DF, Zeidler A, Rotter JI, Yang MC, Modilevsky T, Maclaren NK, She JX.

Hum Mol Genet. 1997 Aug;6(8):1275-82.PMID: 9259273 [PubMed - indexed for MEDLINE]Related articlesFree article

The GENNID Study. A resource for mapping the genes that cause NIDDM.

Raffel LJ, Robbins DC, Norris JM, Boerwinkle E, DeFronzo RA, Elbein SC, Fujimoto W, Hanis CL, Kahn SE, Permutt MA, Chiu KC, Cruz J, Ehrmann DA, Robertson RP, Rotter JI, Buse J.

Diabetes Care. 1996 Aug;19(8):864-72.PMID: 8842605 [PubMed - indexed for MEDLINE]Related articles

Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8.

Luo DF, Buzzetti R, Rotter JI, Maclaren NK, Raffel LJ, Nisticò L, Giovannini C, Pozzilli P, Thomson G, She JX.

Hum Mol Genet. 1996 May;5(5):693-8.PMID: 8733139 [PubMed - indexed for MEDLINE]Related articlesFree article

Association of HLA-DPB1*0301 with IDDM in Mexican-Americans.

Erlich HA, Rotter JI, Chang JD, Shaw SJ, Raffel LJ, Klitz W, Bugawan TL, Zeidler A.

Diabetes. 1996 May;45(5):610-4.PMID: 8621011 [PubMed - indexed for MEDLINE]Related articles

Gorlin syndrome (naevoid basal cell carcinoma syndrome): prenatal detection in a fetus with macrocephaly and ventriculomegaly.

Hogge WA, Blank C, Roochvarg LB, Hogge JS, Wulfsberg EA, Raffel LJ.

Prenat Diagn. 1994 Aug;14(8):725-7.PMID: 7991513 [PubMed - indexed for MEDLINE]Related articles

A multidisciplinary approach to the early detection of ovarian carcinoma: rationale, protocol design, and early results.

Karlan BY, Raffel LJ, Crvenkovic G, Smrt C, Chen MD, Lopez E, Walla CA, Garber C, Cane P, Sarti DA, et al.

Am J Obstet Gynecol. 1993 Sep;169(3):494-501.PMID: 8372851 [PubMed - indexed for MEDLINE]Related articles

Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries.

Leana-Cox J, Levin S, Surana R, Wulfsberg E, Keene CL, Raffel LJ, Sullivan B, Schwartz S.

Am J Hum Genet. 1993 Jun;52(6):1067-73.PMID: 8503441 [PubMed - indexed for MEDLINE]Related articlesFree article

HLA class II alleles and susceptibility and resistance to insulin dependent diabetes mellitus in Mexican-American families.

Erlich HA, Zeidler A, Chang J, Shaw S, Raffel LJ, Klitz W, Beshkov Y, Costin G, Pressman S, Bugawan T, et al.

Nat Genet. 1993 Apr;3(4):358-64.PMID: 7981758 [PubMed - indexed for MEDLINE]Related articles

Transient neonatal galactosaemia identified by newborn screening.

Raffel LJ, Cowan TM, Blitzer MG.

J Inherit Metab Dis. 1993;16(5):894-5. No abstract available. PMID: 8295408 [PubMed - indexed for MEDLINE]Related articles

Prenatal detection of 45,X/46,XX/47,XXX mosaicism through amniocentesis: mosaicism confirmed in cord blood, amnion, and chorion.

Schwartz S, Raffel LJ.

Prenat Diagn. 1992 Dec;12(12):1043-6.PMID: 1283786 [PubMed - indexed for MEDLINE]Related articles

An unusual mosaic karyotype detected through prenatal diagnosis with duplication of 1q and 19p and associated teratoma development.

Schwartz S, Raffel LJ, Sun CC, Waters E.

Teratology. 1992 Oct;46(4):399-404.PMID: 1384156 [PubMed - indexed for MEDLINE]Related articles

The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families.

Raffel LJ, Hitman GA, Toyoda H, Karam JH, Bell GI, Rotter JI.

J Med Genet. 1992 Jul;29(7):447-50.PMID: 1353534 [PubMed - indexed for MEDLINE]Related articlesFree article

HLA-DR and the 5' insulin gene polymorphism in insulin-dependent diabetes.

Raffel LJ, Vadheim CM, Klein R, Moss SE, Riley WJ, Maclaren NK, Rotter JI.

Metabolism. 1991 Dec;40(12):1244-8.PMID: 1961115 [PubMed - indexed for MEDLINE]Related articles

Prenatal ascertainment of an inherited dup(18p) associated with an apparently normal phenotype.

Wolff DJ, Raffel LJ, Ferré MM, Schwartz S.

Am J Med Genet. 1991 Dec 1;41(3):319-21. Review.PMID: 1789286 [PubMed - indexed for MEDLINE]Related articles

De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches.

Schwartz S, Harris M, Ehrenpreis R, Zaslav A, Raffel LJ, Schwartz MF, Lieber E, Cohen MM.

Clin Genet. 1991 Dec;40(6):417-22.PMID: 1778004 [PubMed - indexed for MEDLINE]Related articles

The 5' insulin gene polymorphism and the genetics of vascular complications in type 1 (insulin-dependent) diabetes mellitus.

Raffel LJ, Vadheim CM, Roth MP, Klein R, Moss SE, Rotter JI.

Diabetologia. 1991 Sep;34(9):680-3.PMID: 1955102 [PubMed - indexed for MEDLINE]Related articles

Proximal interstitial deletion of 7q: a case report and review of the literature.

Zackowski JL, Raffel LJ, Blank CA, Schwartz S.

Am J Med Genet. 1990 Jul;36(3):328-32. Review.PMID: 2194394 [PubMed - indexed for MEDLINE]Related articles

A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.

Zackowski JL, Raffel LJ, McDaniel LD, Schwartz S.

Ann Genet. 1990;33(2):113-6.PMID: 2241085 [PubMed - indexed for MEDLINE]Related articles

Recent advances in genetics.

Blitzer MG, Schwartz S, Cowan TM, Raffel LJ.

Md Med J. 1989 Nov;38(11):917-24. Review. No abstract available. PMID: 2685498 [PubMed - indexed for MEDLINE]Related articles

Antenatal detection of cystic hygroma.

Cohen MM, Schwartz S, Schwartz MF, Blitzer MG, Raffel LJ, Mullins-Keene CL, Sun CC, Blakemore KJ.

Obstet Gynecol Surv. 1989 Jun;44(6):481-90. Review.PMID: 2660038 [PubMed - indexed for MEDLINE]Related articles

Chromosomal mosaicism in the Killian/Teschler-Nicola syndrome.

Raffel LJ, Mohandas T, Rimoin DL.

Am J Med Genet. 1986 Aug;24(4):607-11.PMID: 3740095 [PubMed - indexed for MEDLINE]Related articles

Immature renal tissue in colonic wall of patient with caudal regression syndrome.

Sun CC, Raffel LJ, Wright LL, Mergner WJ.

Arch Pathol Lab Med. 1986 Jul;110(7):653-5.PMID: 3013121 [PubMed - indexed for MEDLINE]Related articles

Relationships between the human pepsinogen DNA and protein polymorphisms.

Taggart RT, Samloff IM, Raffel LJ, Graham A, Cass C, Petersen GM, Rotter JI, Skolnick MH, Schwartz CE, Bell GI.

Am J Hum Genet. 1986 Jun;38(6):848-54.PMID: 3014868 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetics, diabetes mellitus heterogeneity, and coronary heart disease.

Rotter JI, Vadheim CM, Raffel LJ, Rimoin DL.

Prog Clin Biol Res. 1984;147:445-78. Review. No abstract available. PMID: 6429664 [PubMed - indexed for MEDLINE]Related articles

Influence of arginine vasotocin on a genetically determined excessive appetite for water in chickens.

Raffel LJ, Buss EG, Glagett CO.

Poult Sci. 1976 Sep;55(5):1834-40.PMID: 995808 [PubMed - indexed for MEDLINE]Related articles